-
1
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
ANDERSON, S., A. T. BANKIER, B. G. BARRELL, M. H. L. DEBRUIJN, A. R. COULSON et al., 1981 Sequence and organization of the human mitochondrial genome. Nature 290: 457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
Debruijn, M.H.L.4
Coulson, A.R.5
-
2
-
-
0023496815
-
Intraspecific phylogeography: The mitochondrial DNA bridge between population genetics and systematics
-
AVISE, J. C., J. ARNOLD, R. M. BALL, E. BERMINGHAM, T. LAMB et al., 1987 Intraspecific phylogeography: the mitochondrial DNA bridge between population genetics and systematics. Annu. Rev. Ecol. Syst. 18: 489-522.
-
(1987)
Annu. Rev. Ecol. Syst.
, vol.18
, pp. 489-522
-
-
Avise, J.C.1
Arnold, J.2
Ball, R.M.3
Bermingham, E.4
Lamb, T.5
-
3
-
-
0028046414
-
Unraveling selection in the mitochondrial genome of Drosophila
-
BALLARD, J. W. O., and M. KREITMAN, 1994 Unraveling selection in the mitochondrial genome of Drosophila. Genetics 138: 757-772.
-
(1994)
Genetics
, vol.138
, pp. 757-772
-
-
Ballard, J.W.O.1
Kreitman, M.2
-
4
-
-
0028348142
-
Neutralism and selection face up to DNA data
-
BROOKFIELD, J. F. Y., and P. M. SHARP, 1994 Neutralism and selection face up to DNA data. Trends Genet. 10: 109-111.
-
(1994)
Trends Genet.
, vol.10
, pp. 109-111
-
-
Brookfield, J.F.Y.1
Sharp, P.M.2
-
5
-
-
0026702249
-
Leber's hereditary optic neuropathy: A model for mitochondrial neurodegenerative diseases
-
BROWN, M. D., A. S. VOLJAVEC, M. T. LOTT, I. MACDONALD and D C. WALLACE, 1992a Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases. FASEB J. 6: 2791-2799.
-
(1992)
FASEB J.
, vol.6
, pp. 2791-2799
-
-
Brown, M.D.1
Voljavec, A.S.2
Lott, M.T.3
Macdonald, I.4
Wallace, D.C.5
-
6
-
-
0026531040
-
Mitochondrial DNA complex I and III mutations associated with Leber's Hereditary Optic Neuropathy
-
BROWN, M. D., A. S. VOLJAVEC, M. T. LOTT, A. TORRONI, C-C. YANG et al., 1992b Mitochondrial DNA complex I and III mutations associated with Leber's Hereditary Optic Neuropathy. Genetics 130: 163-173.
-
(1992)
Genetics
, vol.130
, pp. 163-173
-
-
Brown, M.D.1
Voljavec, A.S.2
Lott, M.T.3
Torroni, A.4
Yang, C.-C.5
-
7
-
-
0345578672
-
Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis
-
BROWN, W. M., 1980 Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis Proc. Natl. Acad. Sci. USA 77: 3605-3609.
-
(1980)
Proc. Natl. Acad. Sci. USA
, vol.77
, pp. 3605-3609
-
-
Brown, W.M.1
-
8
-
-
0023163377
-
Mitochondrial DNA and human evolution
-
CANN, R. L., M. STONEKING and A. C. WILSON, 1987 Mitochondrial DNA and human evolution. Nature 325: 31-36.
-
(1987)
Nature
, vol.325
, pp. 31-36
-
-
Cann, R.L.1
Stoneking, M.2
Wilson, A.C.3
-
9
-
-
0001087283
-
Founder effects and the rate of mitochondrial DNA evolution in Hawaiian Drosophila
-
DESALLE, R., and A. R. TEMPLETON, 1988 Founder effects and the rate of mitochondrial DNA evolution in Hawaiian Drosophila. Evolution 42: 1076-1084.
-
(1988)
Evolution
, vol.42
, pp. 1076-1084
-
-
Desalle, R.1
Templeton, A.R.2
-
10
-
-
0026063965
-
Branching pattern in the evolutionary tree for human mitochondrial DNA
-
DI RIENZO, A., and A. C. WISLON, 1991 Branching pattern in the evolutionary tree for human mitochondrial DNA. Proc. Natl. Acad. Sci. USA 88: 1597-1601.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 1597-1601
-
-
Di Rienzo, A.1
Wislon, A.C.2
-
11
-
-
0025138495
-
Evolution of human mitochondrial DNA: Evidence for departure from a pure neutral model of populations at equilibrium
-
EXCOFFIER, L., 1990 Evolution of human mitochondrial DNA: evidence for departure from a pure neutral model of populations at equilibrium. J. Mol. Evol. 30: 125-139.
-
(1990)
J. Mol. Evol.
, vol.30
, pp. 125-139
-
-
Excoffier, L.1
-
12
-
-
0021062209
-
Mitochondrial DNA evolution in mice
-
FERRIS, S. D., R. D. SAGE, E. M. PRAGER, U. RITTE and A. C. WILSON, 1983 Mitochondrial DNA evolution in mice. Genetics 105: 681-721.
-
(1983)
Genetics
, vol.105
, pp. 681-721
-
-
Ferris, S.D.1
Sage, R.D.2
Prager, E.M.3
Ritte, U.4
Wilson, A.C.5
-
14
-
-
0028127469
-
Substitution processes in molecular evolution. III. Deleterious alleles
-
GILLESPIE, J. H., 1994 Substitution processes in molecular evolution. III. Deleterious alleles. Genetics 138: 943-952.
-
(1994)
Genetics
, vol.138
, pp. 943-952
-
-
Gillespie, J.H.1
-
15
-
-
0023441696
-
Mitochondrial DNA variation and genetic structure in populations of Drosophila melanogaster
-
HALE, L. R., and R. S. SINGH, 1987 Mitochondrial DNA variation and genetic structure in populations of Drosophila melanogaster Mol. Biol. Evol. 4: 622-637.
-
(1987)
Mol. Biol. Evol.
, vol.4
, pp. 622-637
-
-
Hale, L.R.1
Singh, R.S.2
-
16
-
-
0028894410
-
Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs
-
HORAI, S., K. HAYASAKA, R. KONDO, K. TSUGANE and N. TAKAHATA, 1995 Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs. Proc. Natl. Acad. Sci. USA 92: 532-536.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 532-536
-
-
Horai, S.1
Hayasaka, K.2
Kondo, R.3
Tsugane, K.4
Takahata, N.5
-
17
-
-
0023339852
-
A test of neutral molecular evolution based on nucleotide data
-
HUDSON, R. R., M. KREITMAN and M. AGUADE, 1987 A test of neutral molecular evolution based on nucleotide data. Genetics 116: 153-159.
-
(1987)
Genetics
, vol.116
, pp. 153-159
-
-
Hudson, R.R.1
Kreitman, M.2
Aguade, M.3
-
18
-
-
0026757115
-
An ND-6 mitochondrial DNA mutation associated with Leber Hereditary Optic Neuropathy
-
JOHNS, D. R., M. J. NEUFELD and R. D. PARK, 1992 An ND-6 mitochondrial DNA mutation associated with Leber Hereditary Optic Neuropathy. Biochem. Biophys. Res. Comm. 187: 1551-1557.
-
(1992)
Biochem. Biophys. Res. Comm.
, vol.187
, pp. 1551-1557
-
-
Johns, D.R.1
Neufeld, M.J.2
Park, R.D.3
-
19
-
-
0027324226
-
Evolution of the mitochondrial ATPase 6 gene in Drosophila: Unusually high level of polymorphism in D. melanogaster
-
KANEKO, M., Y. SATTA, E. T. MATSURA and S. CHIGUSA, 1993 Evolution of the mitochondrial ATPase 6 gene in Drosophila: unusually high level of polymorphism in D. melanogaster. Genet. Res. 61: 195-204.
-
(1993)
Genet. Res.
, vol.61
, pp. 195-204
-
-
Kaneko, M.1
Satta, Y.2
Matsura, E.T.3
Chigusa, S.4
-
20
-
-
17744413756
-
Model of effectively neutral mutations in which selective constraint is incorporated
-
KIMURA, M., 1979 Model of effectively neutral mutations in which selective constraint is incorporated. Proc. Natl. Acad. Sci. USA 76: 3440-3444.
-
(1979)
Proc. Natl. Acad. Sci. USA
, vol.76
, pp. 3440-3444
-
-
Kimura, M.1
-
22
-
-
0025992003
-
Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)
-
KOBAYASHI, Y., M. Y. MOMOI, K. TOMINAGA, H. SHIMOIZUMI, K. NIHEI et al., 1991 Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS). Am. J. Hum. Genet. 49: 590-599.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 590-599
-
-
Kobayashi, Y.1
Momoi, M.Y.2
Tominaga, K.3
Shimoizumi, H.4
Nihei, K.5
-
23
-
-
0028088717
-
Mitochondrial DNA polymorphism in disease: A possible contributor to respiratory dysfunction
-
LERTRIT, P., R. M. I. KAPSA, M.J. B. JEAN-FRANCOIS, D. THYAGARAJAN, A. S. NOER et al., 1994 Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction. Hum. Mol. Genet. 3: 1973-1981.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1973-1981
-
-
Lertrit, P.1
Kapsa, R.M.I.2
Jean-Francois, M.J.B.3
Thyagarajan, D.4
Noer, A.S.5
-
24
-
-
0026053092
-
Low nucleotide diversity in man
-
LI, W.-H., and L. A. SADLER, 1991 Low nucleotide diversity in man. Genetics 129: 513-523.
-
(1991)
Genetics
, vol.129
, pp. 513-523
-
-
Li, W.-H.1
Sadler, L.A.2
-
25
-
-
0026584717
-
Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains
-
LIN, F.-H., R. LIN, H. M. WISNIEWSKI, Y.-W. HWANG, I. GRUNDKE-IQBAL et al., 1992 Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains. Biochem. Biophys. Res. Comm. 182: 238-246.
-
(1992)
Biochem. Biophys. Res. Comm.
, vol.182
, pp. 238-246
-
-
Lin, F.-H.1
Lin, R.2
Wisniewski, H.M.3
Hwang, Y.-W.4
Grundke-Iqbal, I.5
-
26
-
-
0026409821
-
Normal variants of human mitochondrial DNA and translation products: The building of a reference data base
-
MARZUKI, S., A. S. NOER, P. LERTRIT, D. THYAGARAJAN, R. KAPSA et al , 1991 Normal variants of human mitochondrial DNA and translation products: the building of a reference data base. Hum Genet. 88: 139-145.
-
(1991)
Hum Genet.
, vol.88
, pp. 139-145
-
-
Marzuki, S.1
Noer, A.S.2
Lertrit, P.3
Thyagarajan, D.4
Kapsa, R.5
-
27
-
-
0026428610
-
Adaptive protein evolution at the Adh locus in Drosophila
-
MCDONALD, J. H., and M. KREITMAN, 1991 Adaptive protein evolution at the Adh locus in Drosophila. Nature 351: 652-654.
-
(1991)
Nature
, vol.351
, pp. 652-654
-
-
Mcdonald, J.H.1
Kreitman, M.2
-
28
-
-
0026340064
-
The structure of human mitochondrial DNA variation
-
MERRIWETHER, D. A., A. G. CLARK, S. W. BALLINGER, T. G. SCHURR, H. SOODYALL et al., 1991 The structure of human mitochondrial DNA variation. J. Mol. Evol 33: 543-555.
-
(1991)
J. Mol. Evol
, vol.33
, pp. 543-555
-
-
Merriwether, D.A.1
Clark, A.G.2
Ballinger, S.W.3
Schurr, T.G.4
Soodyall, H.5
-
29
-
-
0028128340
-
Kin selection, social structure, gene flow, and the evolution of chimpanzees
-
MORIN, P A., J. J. MOORE, R. CHAKRABORTY, L. JIN, J. GOODALL et al., 1994 Kin selection, social structure, gene flow, and the evolution of chimpanzees. Science 265: 1193-1201.
-
(1994)
Science
, vol.265
, pp. 1193-1201
-
-
Morin, P.A.1
Moore, J.J.2
Chakraborty, R.3
Jin, L.4
Goodall, J.5
-
30
-
-
0028279173
-
Nonneutral evolution at the mitochondrial NADH dehydrogenase subunit 3 gene in mice
-
NACHMAN, M. W., S. N. BOYER and C. F. AQUADRO, 1994 Nonneutral evolution at the mitochondrial NADH dehydrogenase subunit 3 gene in mice. Proc. Natl. Acad. Sci. USA 91: 6364-6368
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 6364-6368
-
-
Nachman, M.W.1
Boyer, S.N.2
Aquadro, C.F.3
-
31
-
-
0005814023
-
Mathematical model for studying genetic variation in terms of restriction endonucleases
-
NEI, M., and W.-H. LI, 1979 Mathematical model for studying genetic variation in terms of restriction endonucleases Proc. Natl. Acad. Sci. USA 76: 5269-5273.
-
(1979)
Proc. Natl. Acad. Sci. USA
, vol.76
, pp. 5269-5273
-
-
Nei, M.1
Li, W.-H.2
-
32
-
-
0012088802
-
Population size and rate of evolution
-
OHTA, T., 1972 Population size and rate of evolution. J. Mol. Evol. 1: 305-314.
-
(1972)
J. Mol. Evol.
, vol.1
, pp. 305-314
-
-
Ohta, T.1
-
33
-
-
0015722319
-
Slightly deleterious mutant substitutions in evolution
-
OHTA, T., 1973 Slightly deleterious mutant substitutions in evolution. Nature 246: 96-98.
-
(1973)
Nature
, vol.246
, pp. 96-98
-
-
Ohta, T.1
-
34
-
-
0017220894
-
Role of very slightly deleterious mutations in molecular evolution and polymorphism
-
OHTA, T., 1976 Role of very slightly deleterious mutations in molecular evolution and polymorphism. Theor. Popul. Biol. 10: 254-275.
-
(1976)
Theor. Popul. Biol.
, vol.10
, pp. 254-275
-
-
Ohta, T.1
-
35
-
-
0027020232
-
The nearly neutral theory of molecular evolution
-
OHTA, T., 1992 The nearly neutral theory of molecular evolution. Annu. Rev. Ecol. Syst. 23: 263-286.
-
(1992)
Annu. Rev. Ecol. Syst.
, vol.23
, pp. 263-286
-
-
Ohta, T.1
-
36
-
-
0025173452
-
Theoretical study of near neutrality. I. Heterozygosity and rate of mutant substitution
-
OHTA, T., and H. TACHIDA, 1990 Theoretical study of near neutrality. I. Heterozygosity and rate of mutant substitution. Genetics 126: 219-229.
-
(1990)
Genetics
, vol.126
, pp. 219-229
-
-
Ohta, T.1
Tachida, H.2
-
37
-
-
0025915472
-
Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy
-
OZAWA, T., M. TANAKA, S. SUGIYAMA, H. INO, K. OHNO et al., 1991 Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy. Biochem. Biophys. Res. Comm. 177: 518-525.
-
(1991)
Biochem. Biophys. Res. Comm.
, vol.177
, pp. 518-525
-
-
Ozawa, T.1
Tanaka, M.2
Sugiyama, S.3
Ino, H.4
Ohno, K.5
-
38
-
-
0026672905
-
Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease?
-
PETRUZZELLA, V., X. CHEN and E. A. SCHON, 1992 Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease? Biochem. Biophys. Res. Comm. 186: 491-497.
-
(1992)
Biochem. Biophys. Res. Comm.
, vol.186
, pp. 491-497
-
-
Petruzzella, V.1
Chen, X.2
Schon, E.A.3
-
39
-
-
0027995091
-
Thermal habit, metabolic rate and the evolution of mitochondrial DNA
-
RAND, D. M., 1994 Thermal habit, metabolic rate and the evolution of mitochondrial DNA. Trends Ecol. Evol. 9: 125-131.
-
(1994)
Trends Ecol. Evol.
, vol.9
, pp. 125-131
-
-
Rand, D.M.1
-
40
-
-
0027942996
-
Neutral and nonneutral evolution of Drosophila mitochondrial DNA
-
RAND, D. M., M. DORFSMAN and L. M KANN, 1994 Neutral and nonneutral evolution of Drosophila mitochondrial DNA. Genetics 138: 741-756.
-
(1994)
Genetics
, vol.138
, pp. 741-756
-
-
Rand, D.M.1
Dorfsman, M.2
Kann, L.M.3
-
41
-
-
0026548159
-
Population growth makes waves in the distribution of pairwise genetic differences
-
ROGERS, A. R., and H. HARPENDING, 1992 Population growth makes waves in the distribution of pairwise genetic differences. Mol. Biol. Evol. 9: 552-569.
-
(1992)
Mol. Biol. Evol.
, vol.9
, pp. 552-569
-
-
Rogers, A.R.1
Harpending, H.2
-
42
-
-
0023022499
-
Analysis of enzymatically amplified Beta-globin and HLA-DQalpha DNA with allele-specific oligonucleotide probes
-
SAIKI, R. K., T. L. BUGAWAN, G. T. HORN, K. B. MULLIS and H. A. ERLICH, 1986 Analysis of enzymatically amplified Beta-globin and HLA-DQalpha DNA with allele-specific oligonucleotide probes. Nature 324: 163-166.
-
(1986)
Nature
, vol.324
, pp. 163-166
-
-
Saiki, R.K.1
Bugawan, T.L.2
Horn, G.T.3
Mullis, K.B.4
Erlich, H.A.5
-
44
-
-
0026460082
-
Population genetics of polymorphism and divergence
-
SAWYER, S. A., and D. L. HARTL, 1992 Population genetics of polymorphism and divergence. Genetics 132: 1161-1176.
-
(1992)
Genetics
, vol.132
, pp. 1161-1176
-
-
Sawyer, S.A.1
Hartl, D.L.2
-
45
-
-
0022169067
-
Gene flow in natural populations
-
SLATKIN, M., 1985 Gene flow in natural populations. Annu. Rev. Ecol. Syst. 16: 393-430.
-
(1985)
Annu. Rev. Ecol. Syst.
, vol.16
, pp. 393-430
-
-
Slatkin, M.1
-
46
-
-
0025231675
-
Geographic variation in human mitochondrial DNA from Papua New Guinea
-
STONEKING, M., L. B. JORDE, K. BHATIA and A. C WILSON, 1990 Geographic variation in human mitochondrial DNA from Papua New Guinea. Genetics 124: 717-733.
-
(1990)
Genetics
, vol.124
, pp. 717-733
-
-
Stoneking, M.1
Jorde, L.B.2
Bhatia, K.3
Wilson, A.C.4
-
48
-
-
0025862963
-
A study on a nearly neutral mutation model in finite populations
-
TACHIDA, H., 1991 A study on a nearly neutral mutation model in finite populations. Genetics 128: 183-192.
-
(1991)
Genetics
, vol.128
, pp. 183-192
-
-
Tachida, H.1
-
49
-
-
0024313579
-
Statistical method for testing the neutral mutation hypothesis by DNA polymorphism
-
TAJIMA, F., 1989 Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123: 585-595.
-
(1989)
Genetics
, vol.123
, pp. 585-595
-
-
Tajima, F.1
-
50
-
-
0027892073
-
Relaxed natural selection in human populations during the Pleistocene
-
TAKAHATA, N., 1993 Relaxed natural selection in human populations during the Pleistocene. Jpn. J. Genet. 68: 539-547.
-
(1993)
Jpn. J. Genet.
, vol.68
, pp. 539-547
-
-
Takahata, N.1
-
51
-
-
0026587335
-
Mitochondrial genetics: A paradigm for aging and degenerative diseases?
-
WALLACE, D. C., 1992a Mitochondrial genetics: a paradigm for aging and degenerative diseases? Science 256: 628-632.
-
(1992)
Science
, vol.256
, pp. 628-632
-
-
Wallace, D.C.1
-
52
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
WALLACE, D. C , 1992b Diseases of the mitochondrial DNA. Annu. Rev. Biochem. 61: 1175-1212.
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
53
-
-
0028233947
-
Mitochondrial DNA mutations in diseases of energy metabolism
-
WALLACE, D. C., 1994 Mitochondrial DNA mutations in diseases of energy metabolism. J. Bioenerg. Biomembr. 26: 241-250.
-
(1994)
J. Bioenerg. Biomembr.
, vol.26
, pp. 241-250
-
-
Wallace, D.C.1
-
54
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's Hereditary Optic Neuropathy
-
WALLACE, D. C., G. SINGH, M. T. LOTT, J. A. HODGE, T. G. SCHURR et al., 1988 Mitochondrial DNA mutation associated with Leber's Hereditary Optic Neuropathy. Science 242: 1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
-
55
-
-
0000705475
-
Report of the committee on human mitochondrial DNA
-
WALLACE, D. C., M. T. LOTT, A TORRONI and M. D. BROWN, 1993 Report of the committee on human mitochondrial DNA. Genome Priority Rep. 1: 727-757.
-
(1993)
Genome Priority Rep.
, vol.1
, pp. 727-757
-
-
Wallace, D.C.1
Lott, M.T.2
Torroni, A.3
Brown, M.D.4
-
56
-
-
0017886236
-
The homozygosity test of neutrality
-
WATTERSON, G. A., 1978 The homozygosity test of neutrality. Genetics 88: 405-417.
-
(1978)
Genetics
, vol.88
, pp. 405-417
-
-
Watterson, G.A.1
-
57
-
-
0022891291
-
Allelic variation in human mitochondrial genes based on patterns of restriction site polymorphism
-
WHITTAM, T. S., A. G. CLARK, M. STONEKING, R. L. CANN and A. C. WILSON, 1986 Allelic variation in human mitochondrial genes based on patterns of restriction site polymorphism. Proc. Natl. Acad. Sci. USA 83: 9611-9615.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 9611-9615
-
-
Whittam, T.S.1
Clark, A.G.2
Stoneking, M.3
Cann, R.L.4
Wilson, A.C.5
-
58
-
-
0000635613
-
Mitochondrial DNA and two perspectives on evolutionary genetics
-
WILSON, A. C., R. L. CANN, S. M. CARR, M. GEORGE, U. B. GYLLENSTEN et al., 1985 Mitochondrial DNA and two perspectives on evolutionary genetics. Biol. J. Linn. Soc. 26: 375-400.
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(1985)
Biol. J. Linn. Soc.
, vol.26
, pp. 375-400
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Wilson, A.C.1
Cann, R.L.2
Carr, S.M.3
George, M.4
Gyllensten, U.B.5
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